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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >High surface area chromia aerogel efficient catalyst and catalyst support for ethylacetate combustion
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High surface area chromia aerogel efficient catalyst and catalyst support for ethylacetate combustion

机译:高表面积氧化铬气​​凝胶高效催化剂和乙酸乙酯燃烧的催化剂载体

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The effect of dispersion and ensembling mode of chromium oxide nanocrystals in bulk xerogels and aerogels on their performance as well as efficiency of high surface area chromia aerogel as catalysts support were investigated in complete ethylacetate (EA) oxidation. Two series of chromia catalysts with a structure of alpha-Cr2O3 (7-110 m(2) g(-1)) and alpha-CrOOH (230-735 m(2) g(-1)) were tested in EA complete oxidation as a model reaction for VOC combustion. For alpha-Cr2O3, the specific activity increased 3.3 times with decreasing the crystal diameter from similar to100 to 13 nm. For alpha-CrOOH materials, where the surface area was determined by the different packing mode of primary nanoparticles of the same size (3-5 nm), the similar specific rate constants were measured with all the tested samples. The activity of the chromia aerogel (alpha-CrOOH, 630 m(2) g(-1)) was four times higher compared with 0.5% Pt/Al2O3 and 30 times higher relative to 30% Cr2O3/SiO2. Oxidative treatment (O-2) at elevated temperatures converts both phases to CrO2, in case of alpha-Cr2O3-only in the crystals surface layer. In both reduced and oxidized states, high concentration of surface oxygen vacancies were detected in alpha-Cr2O3 and alpha-CrOOH catalysts. A redox cycle Cr(III) []OH <----> 4 Cr(IV)[O]O which determines the catalysts performance at the surface of both types of bulk chromia materials was proposed. Promotion of high surface area chromia aerogel with Pt, Au, Mn and Ce increased its activity in EA complete oxidation by a factor of 1.25-2.7. Addition of Pt, Mn to ceria-promoted chromia aerogel has a significant effect, yielding a high specific rate constant. Promotion with Ce- and Mn-additives improved the efficiency of redox cycle in Cr-aerogel and increased the concentration of surface oxygen vacancies. (C) 2003 Elsevier B.V. All rights reserved. [References: 39]
机译:研究了氧化铬纳米晶体在干凝胶和气凝胶中的分散和聚集方式对其在全乙酸乙酯(EA)氧化中的性能以及高表面积氧化铬气​​凝胶作为催化剂载体的效率的影响。在EA完全氧化中测试了具有α-Cr2O3(7-110 m(2)g(-1))和α-CrOOH(230-735 m(2)g(-1))结构的两个系列氧化铬催化剂作为VOC燃烧的模型反应。对于α-Cr2O3,比活度增加了3.3倍,晶体直径从相似的100纳米减小到13纳米。对于α-CrOOH材料,其表面积由相同大小(3-5 nm)的初级纳米颗粒的不同堆积模式确定,对所有测试样品均测量了相似的比速率常数。氧化铬气凝胶(alpha-CrOOH,630 m(2)g(-1))的活性是0.5%Pt / Al2O3的四倍,相对于30%Cr2O3 / SiO2的活性高30倍。如果仅在晶体表面层中使用α-Cr2O3,则高温下的氧化处理(O-2)会将两相都转化为CrO2。在还原和氧化状态下,在α-Cr2O3和α-CrOOH催化剂中均检测到高浓度的表面氧空位。提出了氧化还原循环Cr(III)[] OH 4 ---- Cr(IV)[O] O,其决定两种类型的块状氧化铬材料表面的催化剂性能。用Pt,Au,Mn和Ce促进高表面积氧化铬气​​凝胶可将其在EA完全氧化中的活性提高1.25-2.7倍。在二氧化铈促进的氧化铬气凝胶中添加Pt,Mn具有显着效果,可产生较高的比速率常数。铈和锰添加剂的促进提高了铬气凝胶中氧化还原循环的效率,并增加了表面氧空位的浓度。 (C)2003 Elsevier B.V.保留所有权利。 [参考:39]

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